免疫学
班级(哲学)
MHC II级
MHC I级
医学
生物
主要组织相容性复合体
计算机科学
免疫系统
人工智能
作者
Malini Raghavan,Natasha Del Cid,Syed M. Rizvi,Larry Robert Peters
标识
DOI:10.1016/j.it.2008.06.004
摘要
The assembly of major histocompatibility complex (MHC) class I molecules with peptides is orchestrated by several assembly factors including the transporter associated with antigen processing (TAP) and tapasin, the endoplasmic reticulum (ER) oxido-reductases ERp57 and protein disulfide isomerase (PDI), the lectin chaperones calnexin and calreticulin, and the ER aminopeptidase (ERAAP). Typically, MHC class I molecules present endogenous antigens to cytotoxic T lymphocytes (CTLs). However, the initiation of CD8(+) T-cell responses against many pathogens and tumors also requires the presentation of exogenous antigens by MHC class I molecules. We discuss recent developments relating to interactions and mechanisms of function of the various assembly factors and pathways by which exogenous antigens access MHC class I molecules.
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